Label: SUPER-SULFUR MAGIC MASK- sulfur paste

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active Ingredients

    Sulfur 10%

    Purpose

    Acne Treatment

  • Uses:

    For the treatment and management of acne. Clears up active acne blemishes and blackheads. Helps to prevent new acne blemishes and blackheads.

  • Warnings

    For external use only.

    When using this product

    Skin irritattion and dryness if more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

    Do not use on 

    broken skin.

    When using this product

    Apply only to areas with acne. If excessive skin irritation develops or increases, discontinue use and consult a doctor. Avoid contact with eyes and mouth.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Clean skin. Apply to affected areas of face. Allow mask to dry for 10-15 minutes and rinse thoroughly with water to remove. Pat dry. Apply 2-3 times per week. If bothersome dryness or peeling occurs, reduce frequency of application.

  • Inactive ingredients

    Water/Aqua, Kaolin, Propanediol, Caprylic/Capric Triglyceride, Glycerin, Magnesium Aluminum Silicate, Arachidyl Alcohol, Behenyl Alcohol, Zinc Oxide, Arachidyl Glucoside, 1.2-Hexanediol, Caprylyl Glycol, Citric Acid, Vaccinium Myrtillus Leaf Cell Extract, Glucose May Contain: Ultramarines CI 77007

  • Package Labeling:

    Outer Package2Inner Package2

  • INGREDIENTS AND APPEARANCE
    SUPER-SULFUR MAGIC MASK 
    sulfur paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83171-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    KAOLIN (UNII: 24H4NWX5CO)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
    VACCINIUM MYRTILLUS LEAF (UNII: Y4U591OU70)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83171-002-0175 mL in 1 TUBE; Type 0: Not a Combination Product07/27/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00607/27/2022
    Labeler - Starface World, Inc. (040399707)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!